Fraicheur Cedre Bleu Antiperspirant And Deodorant Roll-on
Product Images NDC 54235-206

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Fraicheur Cedre Bleu Antiperspirant And Deodorant Roll-on (NDC 54235-206). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Yves Rocher North America Inc. Dba Laboratoire De Biologie Vegetal Yves Rocher, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Back Label (Fraicheur Cedre Bleu Antiperspirant And Deodorant Roll On Back Label)

Back Label (Fraicheur Cedre Bleu Antiperspirant And Deodorant Roll On Back Label)
Drug Facts panel for FRAICHEUR CEDRE BLEU ANTIPERSPIRANT AND DEODORANT ROLL-ON. Lists active ingredient as Aluminum sesquichlorohydrate 15%, purpose as antiperspirant, and use to reduce underarm perspiration. Includes warnings about external use only, avoiding broken skin, and keeping out of reach of children. Directions advise applying as needed to underarms. Non-medicinal ingredients and distributor contact information are also provided.*
FDA Label Image

Front Label (Fraicheur Cedre Bleu Antiperspirant And Deodorant Roll On Front Label)

Front Label (Fraicheur Cedre Bleu Antiperspirant And Deodorant Roll On Front Label)
Label of FRAICHEUR CEDRE BLEU Antiperspirant and Deodorant Roll-on by Yves Rocher North America, showing a botanical illustration. The label includes the product name in multiple languages, volume as 60 ml (2.0 fl. oz.), and the Yves Rocher logo with NPN80004463.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.